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rs1057516868

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057516868(A;T)
Make rs1057516868(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position99862255
GeneAGL
is asnp
is mentioned by
dbSNPrs1057516868
dbSNP (old)rs1057516868
ClinGenrs1057516868
ebirs1057516868
HLIrs1057516868
Exacrs1057516868
Gnomadrs1057516868
Varsomers1057516868
Maprs1057516868
PheGenIrs1057516868
Biobankrs1057516868
1000 genomesrs1057516868
hgdprs1057516868
ensemblrs1057516868
gopubmedrs1057516868
geneviewrs1057516868
scholarrs1057516868
googlers1057516868
pharmgkbrs1057516868
gwascentralrs1057516868
openSNPrs1057516868
23andMers1057516868
23andMe allrs1057516868
SNPshotrs1057516868
SNPdbers1057516868
MSV3drs1057516868
GWAS Ctlgrs1057516868
Max Magnitude0
ClinVar
Risk rs1057516868(T;T)
Alt rs1057516868(T;T)
Reference Rs1057516868(A;A)
Significance Probable-Pathogenic
Disease Glycogen storage disease type III
Variation info
Gene AGL
CLNDBN Glycogen storage disease type III
Reversed 0
HGVS NC_000001.10:g.100327811A>T
CLNSRC
CLNACC RCV000412181.1,